Visible-Light-Mediated [2+2] Photocycloadditions of Alkynes

Visible-light-mediated [2+2] photocycloaddition reaction can be considered an ideal solution due to its green and sustainable properties, and is one of the most efficient methods to synthesize four-membered ring motifs. Although research on the [2+2] photocycloaddition of alkynes is challenging because of the diminished reactivity of alkynes, and the more significant ring strain of the products, remarkable achievements have been made in this field. In this article, we highlight the recent advances in visible-light-mediated [2+2] photocycloaddition reactions of alkynes, with focus on the reaction mechanism and the late-stage synthetic applications. Advances in obtaining cyclobutenes, azetines, and oxetene active intermediates continue to be breakthroughs in this fascinating field of research. Photochemical [2+2] cycloaddition is a universal and straightforward pathway for carbocyclic or heterocyclic organic compounds. In this article, we highlight the most recent advances in visible-light-mediated [2+2] photocycloaddition reactions of alkynes with focus on the reaction mechanism and the late-stage synthetic applications. Advances in obtaining cyclobutenes, azetines, and oxetene intermediates continue to be breakthroughs in this fascinating field of research. image